NDC 41250-001 Meijer Spf 8
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41250 - Meijer Distribution Inc
- 41250-001 - Meijer Spf 8
Product Packages
NDC Code 41250-001-57
Package Description: 295 mL in 1 BOTTLE
Product Details
What is NDC 41250-001?
What are the uses for Meijer Spf 8?
Which are Meijer Spf 8 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Meijer Spf 8 Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- MINERAL OIL (UNII: T5L8T28FGP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PETROLATUM (UNII: 4T6H12BN9U)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- TROLAMINE (UNII: 9O3K93S3TK)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- COCOA BUTTER (UNII: 512OYT1CRR)
- SHEA BUTTER (UNII: K49155WL9Y)
- COCONUT OIL (UNII: Q9L0O73W7L)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARROT (UNII: L56Z1JK48B)
- BANANA (UNII: 4AJZ4765R9)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".